International safety notice
Lot recall of Check-Flo hemostasis assembly / Flexor radial access sets / TriForce peripheral crossing set / Check-Flo introducer (Hausdorf-lock atrial), Cook Medical Europe
Germany / BfArM · DEU · Feb 23, 2017
Key facts
| Title | Lot recall of Check-Flo hemostasis assembly / Flexor radial access sets / TriForce peripheral crossing set / Check-Flo introducer (Hausdorf-lock atrial), Cook Medical Europe |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot recall of Check-Flo hemostasis assembly / Flexor radial access sets / TriForce peripheral crossing set / Check-Flo introducer (Hausdorf-lock atrial), Cook Medical Europe |
| Manufacturer | Lot recall of Check-Flo hemostasis assembly / Flexor radial access sets / TriForce peripheral crossing set / Check-Flo introducer (Hausdorf-lock atrial), Cook Medical Europe |
| Models | G23121, KCFN-6.0-18-23-RA-S-HC, G35596, KCFN-4.0-18-13-RA-HC, G56412, 52499, KCFN-7.0-18-13-RA-HC, G35609, KCFN-5.0-18-7-RA-HC, G35601, KCFN-7.0-18-23-RA-HC, KCFN-5.0-18-13-RA-S-HC and 37 more |
| Date | Feb 23, 2017 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1